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Hypoparathyroidism

Expanded Access Program of Palopegteriparatide in Patients With Hypoparathyroidism

Sponsored by Ascendis Pharma Bone Diseases A/S

About this trial

Last updated a year ago

Study ID

ASNDMAP001

Status

Available

Type

Expanded Access

Placebo

No

Accepting

18-75 Years
18+ Years
All
All

What is this trial about?

To provide palopegteriparatide (TransCon PTH), an investigational parathyroid hormone (PTH) replacement therapy in an expanded access setting for adult patients with hypoparathyroidism who have previously received PTH-treatment, who meet the eligibility criteria for this protocol as described below and have a clear unmet medical need that cannot be adequately treated by a commercial product or a clinical trial.

What are the participation requirements?

Yes

Inclusion Criteria

- Diagnosis of hypoparathyroidism.

- Patients with previous PTH-treatment experience.

- Serum albumin-adjusted calcium level ≥7.8 mg/dL and 25(OH) vitamin D in the normal range within 2 weeks before first dose.

- Body mass index (BMI) 17 - 40 kg/m2.

- Be willing and able to give written informed consent by signing an Institutional Review Board (IRB)-approved Informed Consent Form (ICF).

No

Exclusion Criteria

- Diagnosis of pseudohypoparathyroidism.

- Currently enrolled in an investigational drug or device study or has used an investigational drug or device within 30 days or 5 half-lives (whichever is longer) of Day 1.

- Severe renal impairment (estimated glomerular filtration rate <30 mL/min/1.73m2).

- Increased risk for osteosarcoma, such as those with Paget's disease of bone or unexplained elevations of alkaline phosphatase, hereditary disorders predisposing to osteosarcoma, or with a prior history of substantial external beam or implant radiation therapy involving the skeleton

- Active malignancy within past 2 years excluding successfully resected thyroid carcinoma and non-melanoma skin cancer.

- Severe or decompensated cardiac disease within 26 weeks, including but not limited to class IV or Stage D heart failure, unstable angina, myocardial infarction or uncontrolled arrhythmias.

- Pregnant or lactating females, or females intending to become pregnant.

- Known allergy and/or sensitivity to palopegteriparatide or its excipients or prior PTH therapy.